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References in periodicals archive ?
Clinical and laboratory findings of Niemann-Pick such as hepatosplenomegaly and cytopenia may mask the diagnosis of HLH.
Conditions associated with hepatosplenomegaly like Gaucher disease, hexosaminidase A deficiency, Sandhoff disease, Niemann-Pick disease type C, Wolman disease, the mucopolysaccharidoses.
The initial physical examination did not reveal lymphadenopathy or hepatosplenomegaly.
5[degrees]C) continued, and hepatosplenomegaly developed.
Extra-articular features include subcutaneous nodules, low-grade fever, lymphadenopathy, hepatosplenomegaly, and rarely anterior uveitis.
Spotted fever is rare in children and presence of hemorrhagic rash with fever, hepatosplenomegaly should make one suspect spotted fever.
For example, in Thalassemia there is chronic anemia with Hepatosplenomegaly.
Clinical features include bone marrow failure resulting in pancytopenia, hepatosplenomegaly, blindness secondary to optic nerve compression, hydrocephalus, and other neurological complications.
However, hepatosplenomegaly, which is not often seen in premature infants, has been reported in seven of the eight HLH cases.
Approximately one fifth had hepatosplenomegaly noted on physical exam.
They share common clinical manifestations, including daily spiking fever, typical transient cutaneous rash, arthritis, lymphadenopathy, hepatosplenomegaly and serositis.